Canonical Allele Identifier: CA2574810787
Gene: F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725793C>A , CM000673.2:g.46725793C>A GRCh38
NC_000011.9:g.46747343C>A , CM000673.1:g.46747343C>A GRCh37
NC_000011.8:g.46703919C>A NCBI36
NG_008953.1:g.11601C>A , LRG_551:g.11601C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-66C>A MANE Select ENSP00000308541.5:n.560-66C>A
ENST00000311907.9:c.560-66C>A ENSP00000308541.5:n.560-66C>A
ENST00000442468.1:c.530-66C>A ENSP00000387413.1:n.530-66C>A
ENST00000490274.1:n.340-66C>A
ENST00000530231.5:c.560-66C>A ENSP00000433907.1:n.560-66C>A
NM_000506.3:c.560-66C>A NP_000497.1:n.560-66C>A
NM_000506.4:c.560-66C>A , LRG_551t1:c.560-66C>A NP_000497.1:n.560-66C>A
NM_001311257.1:c.512-66C>A NP_001298186.1:n.512-66C>A
XR_428840.2:n.604-66C>A
XR_428840.4:n.595-66C>A
NM_000506.5:c.560-66C>A MANE Select NP_000497.1:n.560-66C>A
NM_001311257.2:c.512-66C>A NP_001298186.1:n.512-66C>A
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